Reported Jul 19, 2017 · Terminated
The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies…
Icu
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: ICU · 600 N Field Dr · Lake Forest, IL · 60045-4835
Is this the product you have?
- The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are available in single channel and in triple channel pumping mechanism types.
- Lot codes and dates
- List number12391 Serial Number
3,257 of 3,257 codes
138400011384000213840003138400041384000513840006138400071384000813840009138400101384001113840012138400131384001413840015138400161384001713840018138400191384002013840021138400221384002313840024138400251384002613840027138400281384002913840030138400311384003213840033138400341384003513840036138400371384003813840039138400401384004113840042138400431384004413840045138400461384004713840048138400491384005013840051138400521384005313840054138400551384005613840057138400581384005913840060
- List number12391 Serial Number
- Amount recalled
- 214
This recall covers 9 products
The agency filed one notice per product. You are reading one of them; the other 8 are below.
Where it was sold
- Nationwide
Why it was recalled
A possible interruption of therapy when an E321 error code occurs while using the infuser, which is caused by battery issues.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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